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PENAPH Participatory Epidemiology and the Use of Models to Design Control Strategies c/o ILRI, P. O. Box 30709, Nairobi, 00100 Kenya; phone: +254-20 422 3000; fax:+ 254-20 422 3001; email:[email protected]

Participatory epidemiology and the use of models to design control strategies

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Presented by Jeff Mariner at the African Swine Fever Diagnostics, Surveillance, Epidemiology and Control Workshop, Nairobi, Kenya, 20-21 July 2011

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Page 1: Participatory epidemiology and the use of models to design control strategies

PENAPH

Participatory Epidemiology and the Use of Models to Design Control Strategies

c/o ILRI, P. O. Box 30709, Nairobi, 00100 Kenya; phone: +254-20 422 3000; fax:+ 254-20 422 3001; email:[email protected]

Page 2: Participatory epidemiology and the use of models to design control strategies

Participatory Epidemiology

The use of participatory rural appraisal techniques to collect epidemiological

knowledge and intelligence

Presenter
Presentation Notes
Although participatory epidemiology and disease searching is a very new approach, it has already become a major tool in the control of trans-boundary diseases such as rinderpest and contagious bovine pleuropneumonia
Page 3: Participatory epidemiology and the use of models to design control strategies

Participatory Rural Appraisal (PRA)

• Qualitative intelligence gathering process

• Key informants• Problem solving

– Multiple methods– Multiple perspectives– Triangulation

• Best-bet scenarios

Page 4: Participatory epidemiology and the use of models to design control strategies
Page 5: Participatory epidemiology and the use of models to design control strategies

Existing Veterinary Knowledge

• Traditional terms and case definitions

• Clinical presentation• Pathology• Vectors• Reservoirs• Epidemiologic

features Photo: T. Leyland

Page 6: Participatory epidemiology and the use of models to design control strategies

Applications

• Basic Research • Active Surveillance

– Participatory Disease Surveillance (PDS)• Holistic Needs Assessment

– Stakeholders, livelihoods and risk• Impact Assessment

– Participatory Impact Assessment (PIA)– Qualitative and Quantitative

• Institutional change

Page 7: Participatory epidemiology and the use of models to design control strategies

Participatory Disease SurveillancePDS

• Active surveillance done by professionals

• Risk-targeted• High detection rate

– Information networks– Extended time frame

• Sensitive and Specific– Validation processes– Laboratory support

• Timely

Page 8: Participatory epidemiology and the use of models to design control strategies
Page 9: Participatory epidemiology and the use of models to design control strategies

Attributes of PE/PDS Programs

• Flexible approach that allows for discovery• Practitioners are problem-solvers and not enumerators• Strength of the approach lies in its flexible and qualitative

nature• Orients and complements, but does not replace structured

and quantitative methods• Information from diverse sources and methods• Analyzed in an iterative process referred to as

triangulation• Integrates biological testing and quantitative methods

when appropriate to objectives

Page 10: Participatory epidemiology and the use of models to design control strategies

PENAPHParticipatory Epidemiology Network for Animal and

Public Health

c/o ILRI, P. O. Box 30709, Nairobi, 00100 Kenya; phone: +254-20 422 3000; fax:+ 254-20 422 3001; email:[email protected]

• Nine core partners

•Building Surveillance Capacity

• Good Practice Guidelines

• Certification of Training

• Research, Policy and Advocacy

• Pro-Poor and One Health Focus

• Knowledge Exchange

Page 11: Participatory epidemiology and the use of models to design control strategies

Appropriate Combinations of Complimentary Techniques

• Participatory methods• Biological testing• Analytical methods

Persistence as a Function of Initial Herd Immunity

0

100

200

300

400

500

600

700

800

0 20000 40000 60000 80000 100000 120000 140000 160000 180000 200000

Initial Number Recovered (Immune)

Le

ng

th o

f O

utb

reak

(D

ays

)

Page 12: Participatory epidemiology and the use of models to design control strategies

Participatory Approaches to the Mathematical Modelling of

Rinderpest and CBPP

PARC, PACE and CAPE

Page 13: Participatory epidemiology and the use of models to design control strategies

Modelling Objective

• Model agents and lineages as they occurred in pastoral areas of East Africa

• Involve stakeholders at all levels in design and address principal questions of pastoralists and policy-makers– More useful and creates a sense of ownership

• Inform policy dialogue leading to more effective strategies– Targeting interventions and surveillance

Page 14: Participatory epidemiology and the use of models to design control strategies

Data Collection• Evidence-based literature review• Participatory epidemiology – expert opinion

– Mortality, prevalence, clinical course, spatial and temporal patterns and contact structure, estimation of R0

– SSI, proportional piling, matrix scoring, relative prevalence scoring, mapping and event trees

• Serology - Estimation of R0

Page 15: Participatory epidemiology and the use of models to design control strategies
Page 16: Participatory epidemiology and the use of models to design control strategies

“Some of us believe we have rinderpest, but we are not really sure. The disease looks like rinderpest, but it doesn’t kill the

animals. It is rinderpest-like or mild rinderpest.”

Somali elder on lineage 2 rinderpest

El Wak, Somalia 1996

Page 17: Participatory epidemiology and the use of models to design control strategies
Page 18: Participatory epidemiology and the use of models to design control strategies

Modelling Approach

• State-Transition• Stochastic

– Critical Community Size– Fade - Out

• Open Population• @ Risk Software• Input Parameters – Beta Pert Distributions• Single population and multipopulation• Outputs – Probability Distributions

Page 19: Participatory epidemiology and the use of models to design control strategies

E I RSb

μ μ μσμ

β γ α

α = recovery rateb = birth rateβ = effective contact rateγ = latency to infectious rateμ = non-specific mortality rateσ = RP mortality rate

S = SusceptibleE = ExposedI = InfectiousR = Resistant

RP Model Structure

Presenter
Presentation Notes
A very simple epidemic open-population, state-transition disease model with lifelong duration of immunity. This diagram may look familiar to those who have seen the RP model. Animals are born at rate ‘b’ into the Susceptible state. When they become infected they move to the Exposed state by a process governed by the effective contact rate, beta. Animals in the Exposed state are infected but not yet shedding the agent. This is analogous to the latent period. Animals begin shedding and move to the Infectious state at state the latency to infectious rate, gamma. Animals in the Infectious either recover at the rate alpha and move to the Recovered state or they die at the CBPP specific mortality rate, sigma, and drop out of the population. As this is an open population model, a general mortality rate, mu, is assumed and animals die at this rate from all states. Unfortunately, CBBP as simple as RP and we will have to add more states and transitions.
Page 20: Participatory epidemiology and the use of models to design control strategies

ωr

ρ ωv

E I RSb

μ μ μσμ

β γ αr

Q

μ

V

αq

κψ

μ CBPP Model

Presenter
Presentation Notes
Finally, as the dynamics of vaccination induced immunity are very different from the immunity of recovered animals, this is most easily modelled by adding an immune state. Three rate parameters are required: (hit enter key 3 times and define each parameter). Please be aware that this diagram will be on the quiz at the end of the presentation.
Page 21: Participatory epidemiology and the use of models to design control strategies

The Basic Reproductive Number Ro

• Number of secondary cases resulting from one infected animal in susceptible population

• Ro is a feature of both the strain of infectious agent and the host population

Page 22: Participatory epidemiology and the use of models to design control strategies

The Importance of R0

• A measure of the transmission rate • Can be easily estimated from field data

– RP - Herd immunity threshold (1-1/R0)– CBPP - Average of first infection– HPAI – Final fraction size

• Effective contact rate, β, can be calculated from R nought.

• Herd immunity targets

Page 23: Participatory epidemiology and the use of models to design control strategies

Inter-Epidemic PeriodRinderpest in Sudan and Somalia

Page 24: Participatory epidemiology and the use of models to design control strategies

Temporal distribution of reports on rinderpest compatible events by year and interview area

Page 25: Participatory epidemiology and the use of models to design control strategies

So What?• Prevalence of Infection

– 0.1 – 0.2 %– Random clinical surveillance to OIE

standards (1%) not useful– Participatory disease surveillance

• Critical Community Size– ~200,000 head– Target vaccination to high risk populations– Large, remote pastoral communities

• Lineage 2 in Somalia– Modest herd immunity levels could

eradicate

Page 26: Participatory epidemiology and the use of models to design control strategies

Disease Persistence as a Function of the Initial Prevalence of Immunity

0

100

200

300

400

500

600

700

800

0 20 40 60 80 100

Initial Prevalence of Immune (%)

Days

Page 27: Participatory epidemiology and the use of models to design control strategies

Murle

Dinka

Toposa

Jikany Nuer

Lou Nuer

Jie

Niagatom

Gawere Nuer

Bor Dinka

Lotuko/Lopit

Laak Nuer

Boya/Didinga

Anuak

Kachipo

ProvincesRiversCattle Populations

300 0 300 600 Kilometers

N

EW

S

East Nile Cattle Populations

Page 28: Participatory epidemiology and the use of models to design control strategies

Traditional Livestock Exchange

Kachipo

1

2

3

Murle

Toposa

Jie

Presenter
Presentation Notes
Cattle exchange is maintains the integrity of the social fabric. It is a key mechanism for managing risk in a highly uncertain environment. Dowry Loan Exchange Raiding
Page 29: Participatory epidemiology and the use of models to design control strategies

Heterogeneous RP Model for lineage 2 in the Somali Ecosystem

• Four populations• Multiple species

– Parameter values can set independently

• Eight year duration• Cattle and buffaloes• Buffalo R0 ~ 8

Page 30: Participatory epidemiology and the use of models to design control strategies

Four Sub-Population Epidemic Curves from a Heterogeneous Population Model for Rinderpest in Cattle Where the Between

Population Contact Rate is 1% of the Within Population Contact Rate

0

20

40

60

80

100

120

140

0 100 200 300 400 500 600 700

Days

Num

ber I

nfec

tious

Sub-population 1Sub-population 2Sub-population 3Sub-population 4

Page 31: Participatory epidemiology and the use of models to design control strategies

Results Over 2 Years

• Mean mortality 0.85% per year• 34% of iterations ended with a prevalence

of infection of 0.1 to 1%• Maximum prevalence 2%• Final average immunity 26%

Page 32: Participatory epidemiology and the use of models to design control strategies

Eight Year Model η = 0.005 and R = 35%

DurationMean 95th % Max Persistence

(%)

10,000 137 323 603 0

20,000 227 532 1100 0

30,000 329 878 1571 0

40,000 408 948 1915 0

50,000 477 1418 2633 0

100,000 1031 2553 2920 3

Page 33: Participatory epidemiology and the use of models to design control strategies

The Role of Buffaloes

Buffaloes % Immune

Cattle - Day of Last Case

Overall – Day of Last Case

5-15 245 247

15-25 264 269

25-35 261 266

45-55 258 265

55-65 253 260

Page 34: Participatory epidemiology and the use of models to design control strategies

Somali Ecosystem

• Buffalo act as an indicator host and do not contribute to persistence in cattle– Explosive outbreaks of short duration

• Small isolated communities can maintain Lineage 2 for prolonged periods

• Intensive surveillance and time

Page 35: Participatory epidemiology and the use of models to design control strategies

Potential of a Combined Vaccination and Treatment Strategy for CBPP

Scenario Baseline 1/α 75% 1/α 50% 1/α

None 75.4 178 59.6 129 33.2 64

Annual – 5 yr 67.8 130 43.0 79 7.6 24

Biannual – 2 yr 57.2 129 - - 4.4 20

Biannual – 5 yr 35.2 83 8.0 43 0.4 16

Page 36: Participatory epidemiology and the use of models to design control strategies

Indications from the CBPP Modelling

• Eradication not possible with existing vaccine without severe movement control

• The potential impact of treatment is at least great as available vaccines– Private sector and consumer driven application

• Research on treatment regimes merits the same level of attention and investment as vaccine development.

Page 37: Participatory epidemiology and the use of models to design control strategies

Conclusion

• Simple, intuitive models serve as good communications tools for underlying concepts

• Bring diverse information together to be tested as for biological coherence

• Choose between strategy options or identify new options

• Involve beneficiaries and decision-makers from the outset.